Fig. 3From: A novel missense mutation in the MYH7 gene causes an uncharacteristic phenotype of myosin storage myopathy: a case reportPartial electropherograms of the genomic region covering the MYH7 gene, with the representation showing the coding strand. Top. Control subject; Bottom. Patient, carrying variant NM_000257.3: c.1370 T > G (p.Ile457Arg) in a heterozygous status. The location of mutated nucleotide is highlighted in greyBack to article page